4.5 Review

Regulation of alveolar macrophage death in acute lung inflammation

期刊

RESPIRATORY RESEARCH
卷 19, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/s12931-018-0756-5

关键词

Acute lung injury; Macrophages; Cell death; Pyroptosis; Necroptosis; Autophagy

资金

  1. National Institutes of Health [R01-HL-079669, R01HL076179-09]
  2. VA Merit Award [1I01BX002729]
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL079669, R01HL076179] Funding Source: NIH RePORTER
  4. Veterans Affairs [I01BX002729] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Acute lung injury (ALI) and its severe form, known as acute respiratory distress syndrome (ARDS), are caused by direct pulmonary insults and indirect systemic inflammatory responses that result from conditions such as sepsis, trauma, and major surgery. The reciprocal influences between pulmonary and systemic inflammation augments the inflammatory process in the lung and promotes the development of ALI. Emerging evidence has revealed that alveolar macrophage (AM) death plays important roles in the progression of lung inflammation through its influence on other immune cell populations in the lung. Cell death and tissue inflammation form a positive feedback cycle, ultimately leading to exaggerated inflammation and development of disease. Pharmacological manipulation of AM death signals may serve as a logical therapeutic strategy for ALI/ARDS. This review will focus on recent advances in the regulation and underlying mechanisms of AM death as well as the influence of AM death on the development of ALI.

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